AME

N-ACETYLMETHIONINE

Created: 2000-05-11
Last modified:  2024-09-27

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Chemical Details

Formal Charge0
Atom Count25
Chiral Atom Count1
Bond Count24
Aromatic Bond Count0
2D diagram of AME

Chemical Component Summary

NameN-ACETYLMETHIONINE
Systematic Name (OpenEye OEToolkits)(2S)-2-acetamido-4-methylsulfanyl-butanoic acid
FormulaC7 H13 N O3 S
Molecular Weight191.248
TypeL-PEPTIDE NH3 AMINO TERMINUS

Chemical Descriptors

TypeProgram Version Descriptor
SMILESACDLabs10.04O=C(NC(C(=O)O)CCSC)C
SMILESCACTVS3.341CSCC[CH](NC(C)=O)C(O)=O
SMILESOpenEye OEToolkits1.5.0CC(=O)NC(CCSC)C(=O)O
Canonical SMILESCACTVS3.341 CSCC[C@H](NC(C)=O)C(O)=O
Canonical SMILESOpenEye OEToolkits1.5.0 CC(=O)N[C@@H](CCSC)C(=O)O
InChIInChI1.03 InChI=1S/C7H13NO3S/c1-5(9)8-6(7(10)11)3-4-12-2/h6H,3-4H2,1-2H3,(H,8,9)(H,10,11)/t6-/m0/s1
InChIKeyInChI1.03 XUYPXLNMDZIRQH-LURJTMIESA-N

Drug Info: DrugBank

DrugBank IDDB01646 
NameN-Acetylmethionine
Groups experimental
Synonyms
  • Methionamine
  • Nα-acetyl-L-methionine
  • Acetyl-L-methionine
  • L-(N-Acetyl)methionine
  • N-Ac-Met
Categories
  • Amino Acids
  • Amino Acids, Neutral
  • Amino Acids, Peptides, and Proteins
  • Amino Acids, Sulfur
  • Sulfur Compounds
CAS number65-82-7

Drug Targets

NameTarget SequencePharmacological ActionActions
RhodopsinMNGTEGPNFYVPFSNATGVVRSPFEYPQYYLAEPWQFSMLAAYMFLLIVL...unknown
N-acylamino acid racemaseMKLSGVELRRVQMPLVAPFRTSFGTQSVRELLLLRAVTPAGEGWGECVTM...unknown
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682

Related Resource References

Resource NameReference
PubChem 448580
ChEBI CHEBI:21557
CCDC/CSD DADGUK